ELISA Scientist

As an ELISA Scientist I/II , you will be responsible for developing, establishing, validating, and executing bioanalytical methods used to support biopharmaceutical testing. This role requires strong laboratory skills, data analysis capabilities, and a commitment to scientific excellence and regulatory compliance. The ideal candidate has hands-on experience with immunoassays and enjoys working in a collaborative, fast-paced laboratory setting where quality, accuracy, and client service are top priorities. Key Responsibilities Perform and support method development, establishment, transfer, and validation activities for ELISA and multiplex ELISA assays . Execute bioanalytical testing using electrochemiluminescence (ECL) platforms and other immunoassay technologies. Generate, analyze, interpret, and review scientific data to ensure accuracy and compliance with cGMP requirements. Utilize software platforms such as SoftMax Pro and laboratory systems to process and evaluate assay results. Troubleshoot assay performance and identify opportunities for continuous improvement. Prepare technical documentation, protocols, reports, and validation summaries. Train and mentor laboratory personnel on established methods and best laboratory practices. Maintain accurate records in accordance with SOPs, regulatory requirements, and data integrity standards. Work effectively within a Laboratory Information Management System (LIMS). Collaborate with cross-functional teams to ensure projects are completed on schedule and meet client expectations. Support laboratory operations while maintaining a safe, organized, and compliant work environment. Minimum Qualifications Bachelor's degree in Biology, Biochemistry, Biotechnology, Cell Biology, Immunology, or a related scientific discipline. 0-4+ years of relevant academic or industry laboratory experience. Authorization to work in the United States without current or future sponsorship. Preferred Qualifications Experience performing ELISA, multiplex ELISA, MSD, or other ligand-binding assays. Knowledge of bioassay development, qualification, and validation. Familiarity with cGMP, GLP, or other regulated laboratory environments. Experience supporting biologics, therapeutic proteins, antibodies, vaccines, or cell- and immuno-based assays. Proficiency with laboratory data analysis software and Microsoft Office applications. Excellent organizational, problem-solving, and communication skills. Ability to manage multiple priorities while maintaining a high level of accuracy and attention to detail. Schedule Full-time | Monday-Friday | 8:00 AM-4:30 PM Additional hours may be required based on project and client needs. Benefits Eurofins offers a comprehensive benefits package, including: Medical, dental, and vision coverage Company-paid life and disability insurance 401(k) with company match Paid vacation and holidays Employee assistance programs Career development and advancement opportunities Candidates living within a commutable distance of Columbia, MO are encouraged to apply. Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.